Canonical Allele Identifier: CA491489135
Gene: CYP1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.75042088G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749747G>A , CM000677.2:g.74749747G>A GRCh38
NC_000015.9:g.75042088G>A , CM000677.1:g.75042088G>A GRCh37
NC_000015.8:g.72829141G>A NCBI36
NG_008431.1:g.32206G>A
NG_008431.2:g.32206G>A
NG_061543.1:g.5903G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.9G>A MANE Select ENSP00000342007.4:p.Leu3=
ENST00000343932.4:c.9G>A ENSP00000342007.4:p.Leu3=
NM_000761.4:c.9G>A NP_000752.2:p.Leu3=
NM_000761.5:c.9G>A MANE Select NP_000752.2:p.Leu3=
Search 100 bp 5'
Search 100 bp 3'